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Clinical Trial Summary

The purpose of this study is to assess shoulder pain at rest (average over the last 24 hours) assessed by visual analogue scale from 0 to 100mm on Day 1.


Clinical Trial Description

This is an interventional, comparative, controlled, randomized, single-blind study (the patient will be blinded to the result of the randomization, unlike the investigator) and single-center. Comparative prospective cohort study of laparoscopic surgery with the addition of specific non-surgical interventions aimed at preventing postoperative shoulder pain (use of local intraperitoneal anesthetics, alveolar recruitment maneuver and compression maneuver abdominal) versus without specific interventions aimed at preventing post-operative shoulder pain. All patients will benefit from Transversus Abdominis Plane block with multimodal analgesia provided in the usual setting of laparoscopic surgery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06039761
Study type Interventional
Source GCS Ramsay Santé pour l'Enseignement et la Recherche
Contact Fabien DECHANET, MD
Phone 6 12 85 91 37
Email dechanet.fabien@hotmail.fr
Status Recruiting
Phase N/A
Start date December 13, 2023
Completion date September 30, 2024

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